TNSN03076A1 - NOVEL SPIRO-TRICYCLIC DERIVATIVES AND THEIR USE AS PHOSPHO-DIESTERASE-7 INHIBITORS - Google Patents
NOVEL SPIRO-TRICYCLIC DERIVATIVES AND THEIR USE AS PHOSPHO-DIESTERASE-7 INHIBITORSInfo
- Publication number
- TNSN03076A1 TNSN03076A1 TNPCT/EP2002/003594A TNSN03076A TNSN03076A1 TN SN03076 A1 TNSN03076 A1 TN SN03076A1 TN SN03076 A TNSN03076 A TN SN03076A TN SN03076 A1 TNSN03076 A1 TN SN03076A1
- Authority
- TN
- Tunisia
- Prior art keywords
- inhibitors
- diesterase
- phospho
- tricyclic derivatives
- novel spiro
- Prior art date
Links
- 239000002606 phosphodiesterase VII inhibitor Substances 0.000 title abstract 2
- 101100407335 Dictyostelium discoideum pde7 gene Proteins 0.000 abstract 1
- 229940123304 Phosphodiesterase 7 inhibitor Drugs 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/80—Oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Virology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Neurosurgery (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
L'invention propose des composés qui sont des inhibiteurs de PDE7, répondant aux formules (I),(II),(III) suivantes dans lesquelles X1, X2, X3, X4, X, Y, Z, A et Z1 ....DANS LAQUELLE X1, X2, X3, X4, X, Y, Z, A ET Z1 REPONDENT AUX DEFINITIONS FIGURANT DANS LA DESCRIPTION, DES PROCEDES POUR LEUR PREPARATION ET LEUR UTILISATION POUR LE TRAITEMENT D'AFFECTIONS POUR LESQUELLES UNE THERAPIE AVEC UN INHIBITEUR DE PDE7 EST INTRESSANTE.The invention provides compounds which are PDE7 inhibitors, corresponding to the following formulas (I), (II), (III) in which X1, X2, X3, X4, X, Y, Z, A and Z1 ... IN WHICH X1, X2, X3, X4, X, Y, Z, A AND Z1 MEET THE DEFINITIONS APPEARING IN THE DESCRIPTION, METHODS FOR THEIR PREPARATION AND THEIR USE FOR THE TREATMENT OF CONDITIONS FOR WHICH THERAPY WITH AN INHIBITOR OF PDE7 IS INTERESTING.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP2001/003355 WO2002076953A1 (en) | 2001-03-21 | 2001-03-21 | New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TNSN03076A1 true TNSN03076A1 (en) | 2005-12-23 |
Family
ID=8164349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNPCT/EP2002/003594A TNSN03076A1 (en) | 2001-03-21 | 2002-03-18 | NOVEL SPIRO-TRICYCLIC DERIVATIVES AND THEIR USE AS PHOSPHO-DIESTERASE-7 INHIBITORS |
Country Status (46)
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1400244A1 (en) * | 2002-09-17 | 2004-03-24 | Warner-Lambert Company LLC | New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors |
| GB0230195D0 (en) * | 2002-12-24 | 2003-02-05 | Biofocus Plc | Compound Libraries |
| EA200701782A3 (en) | 2003-04-24 | 2008-04-28 | Инсайт Корпорейшн | DERIVATIVES OF AZASPYROALKANES AS METHOD PROTEASIS INHIBITORS |
| JP2006219374A (en) | 2003-06-13 | 2006-08-24 | Daiichi Asubio Pharma Co Ltd | Imidazotriazinone derivatives having PDE7 inhibitory action |
| JP2006219373A (en) | 2003-06-13 | 2006-08-24 | Daiichi Asubio Pharma Co Ltd | Pyridinylpyrazolopyrimidinone derivatives having PDE7 inhibitory action |
| JP2007501822A (en) * | 2003-08-12 | 2007-02-01 | エフ．ホフマン−ラ ロシュ アーゲー | Spiro-substituted tetrahydroquinazolines as corticotropin releasing factor (CRF) antagonists |
| EP2433943B1 (en) | 2004-07-01 | 2013-09-11 | Daiichi Sankyo Company, Limited | Intermediates for thienopyrazole derivatives having PDE7 inhibitory activity |
| WO2006092692A1 (en) * | 2005-03-01 | 2006-09-08 | Pfizer Limited | Use of combinations of pde7 inhibitors and alpha-2-delty ligands for the treatment of neuropathic pain |
| AU2006219643A1 (en) * | 2005-03-01 | 2006-09-08 | Pfizer Limited | Use of PDE7 inhibitors for the treatment of neuropathic pain |
| GB0504209D0 (en) * | 2005-03-01 | 2005-04-06 | Pfizer Ltd | New use of PDE7 inhibitors |
| KR100680497B1 (en) * | 2005-07-25 | 2007-02-08 | 엘지전자 주식회사 | How a terminal connects to an access point in a local area communication system |
| AU2006282896A1 (en) | 2005-08-26 | 2007-03-01 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
| EP2258357A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
| WO2007047978A2 (en) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
| JP2009513672A (en) | 2005-10-31 | 2009-04-02 | ブレインセルス，インコーポレイティド | GABA receptor-mediated regulation of neurogenesis |
| US20070225217A1 (en) | 2005-11-09 | 2007-09-27 | Combinatorx, Incorporated | Methods, compositions, and kits for the treatment of medical conditions |
| WO2007063391A2 (en) | 2005-12-02 | 2007-06-07 | Pfizer Limited | Spirocyclic quinazoline derivatives as pde7 inhibitors |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| EP2377531A2 (en) | 2006-05-09 | 2011-10-19 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| MX2008014320A (en) | 2006-05-09 | 2009-03-25 | Braincells Inc | 5 ht receptor mediated neurogenesis. |
| US7998971B2 (en) * | 2006-09-08 | 2011-08-16 | Braincells Inc. | Combinations containing a 4-acylaminopyridine derivative |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| US8637528B2 (en) | 2007-03-27 | 2014-01-28 | Omeros Corporation | Use of PDE7 inhibitors for the treatment of movement disorders |
| CN101917992A (en) | 2007-03-27 | 2010-12-15 | 奥默罗斯公司 | Use of PDE7 inhibitors for the treatment of movement disorders |
| US20100216823A1 (en) * | 2007-05-24 | 2010-08-26 | Pfizer Inc. | Spirocyclic Derivatives |
| WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
| US9220715B2 (en) | 2010-11-08 | 2015-12-29 | Omeros Corporation | Treatment of addiction and impulse-control disorders using PDE7 inhibitors |
| EP4275752A3 (en) | 2010-11-08 | 2024-02-21 | Omeros Corporation | Treatment of addiction and impulse-control disorders using pde7 inhibitors |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| WO2013106547A1 (en) | 2012-01-10 | 2013-07-18 | President And Fellows Of Harvard College | Beta-cell replication promoting compounds and methods of their use |
| ES2984771T3 (en) | 2012-06-13 | 2024-10-31 | Incyte Holdings Corp | Substituted tricyclic compounds as FGFR inhibitors |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| EA035095B1 (en) | 2013-04-19 | 2020-04-27 | Инсайт Холдингс Корпорейшн | Bicyclic heterocycles as fgfr inhibitors |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (en) | 2015-02-20 | 2017-12-26 | Incyte Corp | BICYCLIC HETEROCYCLES USED AS FGFR4 INHIBITORS |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| EA038045B1 (en) | 2015-02-20 | 2021-06-28 | Инсайт Корпорейшн | Bicyclic heterocycles as fgfr inhibitors |
| JP7037483B2 (en) * | 2015-12-16 | 2022-03-16 | チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッド | Pyrimidone [1,2-a] pyrimidone analogs, their crystal forms, their intermediates, and methods of their manufacture. |
| AR111960A1 (en) | 2017-05-26 | 2019-09-04 | Incyte Corp | CRYSTALLINE FORMS OF A FGFR INHIBITOR AND PROCESSES FOR ITS PREPARATION |
| CN107382976A (en) * | 2017-07-04 | 2017-11-24 | 孙秀芹 | A kind of compound and preparation method and application for treating pelvic infecton |
| CA3069432A1 (en) * | 2017-07-12 | 2019-01-17 | Dart Neuroscience, Llc | Substituted benzoxazole and benzofuran compounds as pde7 inhibitors |
| RS66310B1 (en) | 2018-05-04 | 2025-01-31 | Incyte Corp | Solid forms of an fgfr inhibitor and processes for preparing the same |
| US11174257B2 (en) | 2018-05-04 | 2021-11-16 | Incyte Corporation | Salts of an FGFR inhibitor |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| PH12022550892A1 (en) | 2019-10-14 | 2023-05-03 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| AU2020395185A1 (en) | 2019-12-04 | 2022-06-02 | Incyte Corporation | Derivatives of an FGFR inhibitor |
| EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| JP2024513575A (en) | 2021-04-12 | 2024-03-26 | インサイト・コーポレイション | Combination therapy including FGFR inhibitor and Nectin-4 targeting agent |
| WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| TW202313610A (en) | 2021-06-09 | 2023-04-01 | 美商英塞特公司 | Tricyclic heterocycles as fgfr inhibitors |
| CN119768172A (en) | 2022-08-18 | 2025-04-04 | 米托迪治愈有限责任公司 | Use of therapeutic agents having phosphodiesterase-7 inhibitory activity in the treatment and prevention of diseases associated with chronic fatigue, exhaustion and/or exertion intolerance |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5815979A (en) | 1981-07-11 | 1983-01-29 | Kyowa Hakko Kogyo Co Ltd | Novel piperidine derivatives and their production method |
| US4764512A (en) | 1986-08-27 | 1988-08-16 | Rorer Pharmaceutical Corporation | Benzodiazinone-pyridone compounds, cardiotonic compositions including the same, and their uses |
| GR1000821B (en) * | 1988-11-22 | 1993-01-25 | Tanabe Seiyaku Co | Process for preparing quinazolinone derivatives |
| US5578593A (en) * | 1992-12-11 | 1996-11-26 | Merck & Co., Inc. | Spiro piperidines and homologs promote release of growth hormone |
| HUT72076A (en) | 1992-12-11 | 1996-03-28 | Merck & Co Inc | Process for preparing spiro piperidines and homologs which promote release of growth hormone and pharmaceutical compositions containing them |
| US5602143A (en) * | 1994-12-08 | 1997-02-11 | Allergan | Method for reducing intraocular pressure in the mammalian eye by administration of guanylate cyclase inhibitors |
| BR9610988A (en) * | 1995-10-17 | 1999-04-06 | Astra Pharma Prod | Composite use of the same pharmaceutical formulation and process for producing the compound |
| CN1205008A (en) * | 1996-08-30 | 1999-01-13 | 协和发酵工业株式会社 | Imidazoquinazoline derivatives |
| CN1179753C (en) | 1999-05-04 | 2004-12-15 | 惠氏公司 | Contraceptive composition containing antiprogestin and progestin |
| US6358948B1 (en) * | 1999-05-04 | 2002-03-19 | American Home Products Corporation | Quinazolinone and benzoxazine derivatives as progesterone receptor modulators |
| WO2000066560A1 (en) * | 1999-05-04 | 2000-11-09 | American Home Products Corporation | Quinazolinone and benzoxazine derivatives as progesterone receptor modulators |
| US6509334B1 (en) | 1999-05-04 | 2003-01-21 | American Home Products Corporation | Cyclocarbamate derivatives as progesterone receptor modulators |
| US6498154B1 (en) | 1999-05-04 | 2002-12-24 | Wyeth | Cyclic regimens using quinazolinone and benzoxazine derivatives |
| AU2274101A (en) | 1999-12-21 | 2001-07-03 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
| UA73119C2 (en) | 2000-04-19 | 2005-06-15 | American Home Products Corpoir | Derivatives of cyclic thiocarbamates, pharmaceutical composition including noted derivatives of cyclic thiocarbamates and active ingredients of medicines as modulators of progesterone receptors |
-
2001
- 2001-03-21 AP APAP/P/2003/002857A patent/AP1699A/en active
- 2001-03-21 WO PCT/EP2001/003355 patent/WO2002076953A1/en not_active Ceased
-
2002
- 2002-03-05 TW TW091104028A patent/TWI267509B/en not_active IP Right Cessation
- 2002-03-18 GE GE5294A patent/GEP20053631B/en unknown
- 2002-03-18 EP EP07104642A patent/EP1801106A3/en not_active Withdrawn
- 2002-03-18 MY MYPI20020954A patent/MY142045A/en unknown
- 2002-03-18 EA EA200300906A patent/EA006815B1/en unknown
- 2002-03-18 WO PCT/EP2002/003594 patent/WO2002074754A1/en not_active Ceased
- 2002-03-18 AT AT02732544T patent/ATE367381T1/en not_active IP Right Cessation
- 2002-03-18 RS YUP-740/03A patent/RS50429B/en unknown
- 2002-03-18 DK DK02732544T patent/DK1373224T3/en active
- 2002-03-18 CA CA002441313A patent/CA2441313C/en not_active Expired - Fee Related
- 2002-03-18 SI SI200230587T patent/SI1373224T1/en unknown
- 2002-03-18 NZ NZ527847A patent/NZ527847A/en unknown
- 2002-03-18 AU AU2002304800A patent/AU2002304800B2/en not_active Ceased
- 2002-03-18 ES ES02732544T patent/ES2288552T3/en not_active Expired - Lifetime
- 2002-03-18 OA OA1200300226A patent/OA12454A/en unknown
- 2002-03-18 UA UA2003098601A patent/UA74243C2/en unknown
- 2002-03-18 KR KR1020037012247A patent/KR100617435B1/en not_active Expired - Fee Related
- 2002-03-18 HR HR20030740A patent/HRP20030740A2/en not_active Application Discontinuation
- 2002-03-18 EP EP02732544A patent/EP1373224B1/en not_active Expired - Lifetime
- 2002-03-18 CN CNB028069714A patent/CN100447136C/en not_active Expired - Fee Related
- 2002-03-18 SK SK1156-2003A patent/SK11562003A3/en not_active Application Discontinuation
- 2002-03-18 TN TNPCT/EP2002/003594A patent/TNSN03076A1/en unknown
- 2002-03-18 PT PT02732544T patent/PT1373224E/en unknown
- 2002-03-18 EE EEP200300459A patent/EE200300459A/en unknown
- 2002-03-18 CZ CZ20032451A patent/CZ20032451A3/en unknown
- 2002-03-18 DE DE60221233T patent/DE60221233T2/en not_active Expired - Lifetime
- 2002-03-18 MX MXPA03008485A patent/MXPA03008485A/en active IP Right Grant
- 2002-03-18 JP JP2002573763A patent/JP4086663B2/en not_active Expired - Fee Related
- 2002-03-18 BR BR0208192-0A patent/BR0208192A/en not_active IP Right Cessation
- 2002-03-18 HU HU0303637A patent/HUP0303637A3/en unknown
- 2002-03-18 IL IL15765902A patent/IL157659A0/en active IP Right Grant
- 2002-03-18 PL PL02367058A patent/PL367058A1/en not_active Application Discontinuation
- 2002-03-19 US US10/101,996 patent/US20020198198A1/en not_active Abandoned
- 2002-03-20 SV SV2002000925A patent/SV2003000925A/en not_active Application Discontinuation
- 2002-03-20 GT GT200200053A patent/GT200200053A/en unknown
- 2002-03-20 PA PA20028541601A patent/PA8541601A1/en unknown
- 2002-03-20 AR ARP020100993A patent/AR033617A1/en active IP Right Grant
- 2002-03-20 PE PE2002000212A patent/PE20021010A1/en not_active Application Discontinuation
-
2003
- 2003-08-25 ZA ZA200306601A patent/ZA200306601B/en unknown
- 2003-08-27 EC EC2003004750A patent/ECSP034750A/en unknown
- 2003-08-28 IL IL157659A patent/IL157659A/en not_active IP Right Cessation
- 2003-08-29 IS IS6934A patent/IS2529B/en unknown
- 2003-08-29 CU CU20030188A patent/CU23218A3/en not_active IP Right Cessation
- 2003-09-12 MA MA27310A patent/MA27001A1/en unknown
- 2003-09-17 BG BG108181A patent/BG108181A/en unknown
- 2003-09-19 NO NO20034187A patent/NO326086B1/en not_active IP Right Cessation
-
2004
- 2004-05-24 US US10/852,404 patent/US7214676B2/en not_active Expired - Fee Related
-
2006
- 2006-10-20 US US11/551,687 patent/US20070049558A1/en not_active Abandoned
-
2007
- 2007-08-30 CY CY20071101121T patent/CY1106829T1/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TNSN03076A1 (en) | NOVEL SPIRO-TRICYCLIC DERIVATIVES AND THEIR USE AS PHOSPHO-DIESTERASE-7 INHIBITORS | |
| EP1673078A4 (en) | BENZYLETHER AND BENZYLAMINO BETA-SECRETASE INHIBITORS FOR THE TREATMENT OF ALZHEIMER'S DISEASE | |
| ATE443043T1 (en) | PHENYLCARBOXAMIDE AS A BETA-SECRETASE INHIBITOR FOR THE TREATMENT OF ALZHEIMER'S | |
| MA26697A1 (en) | NOVEL GSK-3 INHIBITOR COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| EP1443905A4 (en) | COMPOSITIONS FOR ORAL GENE THERAPY AND METHODS OF USE THEREOF | |
| TNSN03130A1 (en) | HIV PROTEASE INHIBITORS, COMPOSITIONS CONTAINING THEM, PHARMACEUTICAL USES THEREOF AND MATERIALS FOR THEIR SYNTHESIS | |
| PT966465E (en) | IMFDH ENZYME INHIBITORS | |
| MA27608A1 (en) | HYDROXYETHYLAMINE DERIVATIVES FOR THE TREATMENT OF ALZHEIMER'S DISEASE | |
| TNSN01091A1 (en) | NOVEL BICYCLIC DERIVATIVES, COMPOSITIONS CONTAINING THEM AND THEIR USE FOR THE TREATMENT OF ABNORMAL CELL GROWTH | |
| TNSN02021A1 (en) | NOVEL BENZIMIDAZOLE DERIVATIVES AND COMPOSITIONS CONTAINING THEM | |
| TNSN02008A1 (en) | NEW MMP INHIBITOR ISOPHTHALIC ACID DERIVATIVES AND COMPOSITIONS CONTAINING THEM | |
| EA199700043A1 (en) | ESTROGEN AGENTS | |
| DE60324183D1 (en) | Aryl-, aryloxy- und alkyloxysubstituierte 1h-indol-3-yl-glyoxylsäurederivateals inhibitoren des plasminogenaktivatorinhibitors-1 (pai-1) | |
| TNSN02022A1 (en) | NEW ANTI-INFLAMMATORY TRIAZOLOPYRIDINES, AND COMPOSITIONS CONTAINING THEM | |
| TR199901191T2 (en) | Use of benzamidoaldehydes as cysteine protease inhibitors. | |
| NO995543L (en) | Mono esters from probukol for the treatment of cardiovascular and inflammatory disease | |
| ATE517861T1 (en) | BENZYL ETHER AND BENZYLAMIN COMPOUNDS AS INHIBITORS OF BETA-SECRETASE FOR THE TREATMENT OF ALZHEIMER'S DISEASE | |
| EP1480658A4 (en) | METHODS FOR TREATING VASCULAR DISEASE | |
| EP1379251A4 (en) | ACTIVITY INHIBITORS OF THE AKT ENZYME | |
| TNSN99028A1 (en) | NOVEL NHE-1 INHIBITOR COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| ATE372334T1 (en) | PHENYLPYRAZOLE DERIVATIVES AS VISION INHIBITORS | |
| TNSN00121A1 (en) | NEW METALLOPROTEASE INHIBITOR COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| DE60327999D1 (en) | AZOLYLAMINOAZINES AS INHIBITORS OF PROTEIN KINASES | |
| ATE527261T1 (en) | 7-ARYL-3,9-DIAZABICYCLOÄ3.3.1ÜNONE-6-EN DERIVATIVES AND THEIR USE AS RENIN INHIBITORS FOR THE TREATMENT OF HYPERTENSION, CARDIOVASCULAR DISEASES AND KIDNEY DISEASES | |
| DK0946502T3 (en) | Sulfonamide inhibitors for the interleukin-1beta converting enzyme |